Job Description
Job Title: Siemens MES – Opcenter Engineer
Location: Singapore
Employment Type: Full‑time
About the Role
We are looking for experienced professionals with 5+ years of pharmaceutical industry experience to join our team in Singapore. The role focuses on implementing and supporting Siemens MES – Opcenter solutions for life sciences manufacturing, ensuring compliance, validation, and operational excellence.
Key Responsibilities
- Configure and implement Siemens MES – Opcenter modules in pharma manufacturing environments.
- Lead and support CSV (Computer System Validation) activities, including deviation handling, change control, and documentation.
- Develop and maintain operating plans and validation protocols.
- Collaborate with QA, Tech Control, and Document Control teams to ensure compliance with GMP and regulatory standards.
- Utilize tools such as Kneat for validation and compliance documentation.
- Provide technical support, troubleshoot issues, and contribute to continuous improvement initiatives.
Requirements
- Bachelor’s degree in Engineering, Computer Science, or related discipline.
- Minimum 5 years of experience in pharmaceutical manufacturing or life sciences projects.
- Proven expertise in MES (preferably Siemens Opcenter).
- Strong knowledge of CSV, deviation writing, and change control processes.
- Familiarity with Kneat or similar compliance tools is a plus.
- Excellent communication, documentation, and stakeholder management skills.
- Ability to work independently and in cross‑functional teams.
Employment Details
- Level: Mid‑Senior
- Availability: Immediate/ASAP
Why Join Us
- Work on cutting‑edge MES projects in the pharmaceutical sector.
- Gain exposure to global compliance and validation standards.
- Be part of a collaborative, growth‑oriented environment with career progression opportunities.
